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1 gulates GLUT1-mediated glucose transport via stomatin.
2  3, flotillin-1 and -2, peroxiredoxin-2, and stomatin.
3 s overall approximately 20% similar to human stomatin.
4 ning these three components is equivalent to stomatin.
5 s a close homologue of the mammalian protein stomatin.
6 t does contain an orthologue of human band 7 stomatin, a protein known to oligomerize, associate with
7                                 In contrast, stomatin accelerated the desensitization rate of ASIC2 a
8                                    Moreover, stomatin altered the function of ASIC channels.
9 of the microstome to an inducer contained in stomatin, an exudate of the prey.
10      UNC-1 shows extensive homology to human stomatin, an integral membrane protein thought to regula
11 sterol and major raft proteins flotillin and stomatin and contain low levels of cytoskeleton, all cha
12 e switch is mediated by the membrane protein stomatin and is an evolutionary adaptation to vitamin C
13                                 Prohibitins, stomatins, and a group of plant defense response genes a
14 onserved in evolution and P. falciparum (Pf) stomatin appears to be a prokaryotic-like molecule.
15 ved in proliferation and cell cycle control, stomatins are involved in ion channel regulation, and th
16                                              Stomatins are members of a large protein family conserve
17                                This revealed stomatin as a potential gene target, which has roles in
18                                 We find that Stomatin assembles into a 16-subunit ring-shaped homo-ol
19                                        Human stomatin (band 7.2b) is a 31-kDa erythrocyte membrane pr
20                                              Stomatins belong to the band-7 protein family, a diverse
21                      These data suggest that stomatin binds to and alters the gating of ASICs.
22 ot a lipid biosynthetic enzyme, depletion of stomatin causes cells to change their lipidomes.
23 s report describes the cloning of the murine stomatin chromosomal gene, determination of its genomic
24                                We found that stomatin co-immunoprecipitated and co-localized with ASI
25 o-electron microscopy structure of the human Stomatin complex in a native membrane environment.
26                                    Silencing stomatin decreased A. phagocytophilum colonization in Ix
27                     There are five mammalian stomatin-domain genes, all of which encode peripheral me
28 ersity of signaling protein genes, including stomatin (Epb7.2), S100A5, Ddit3, Sirt2, CD81, Sdc2, Omp
29 Its product, podocin, is a new member of the stomatin family, which consists of hairpin-like integral
30 ing that these features are conserved in the stomatin family.
31                              Among these are Stomatin-family proteins, which are known to influence m
32  raft-associated integral membrane proteins (stomatin, flotillin 1, and flotillin 2), extracellular s
33 oncordance between the exon structure of the stomatin gene and the locations of three domains predict
34                                          The stomatin gene is encoded by seven exons spread over appr
35 s identify a novel and unusual member of the stomatin gene superfamily that interacts with the periph
36                                              Stomatin has multiple contacts with the plasma membrane
37 be linked to the mechanosensitive channel by stomatin-homologous MEC-2.
38                   In Caenorhabditis elegans, stomatin homologs interact with DEG/ENaC channels, which
39                                          Two stomatin homologs, MEC-2 and UNC-24, interact with the M
40 ng and characterization of a new and unusual stomatin homologue, human SLP-2 (stomatin-like protein 2
41                                     A second stomatin homologue, termed SLP-1, has been identified in
42 )-terminal hydrophobic domain found in other stomatin homologues and (unlike stomatin) is fully extra
43 on of exogenous phosphatidylcholines rescues stomatin-induced defects.
44                  Therefore, we asked whether stomatin interacts with and modulates the function of AS
45                      These data suggest that stomatin interfaces with lipid metabolism.
46                                              Stomatin is a poorly understood integral membrane protei
47                                              Stomatin is an integral membrane protein found in lipid/
48    Here, we report that the membrane protein stomatin is involved in the cytokinesis step of cell div
49 rom patients with hereditary stomatocytosis, stomatin is not linked to this disorder.
50                                    Mammalian stomatin is thought to interact with an as-yet-unknown i
51 " revealed that the ATF6-regulated nature of stomatin is unique to blood-feeding arthropods.
52 und in other stomatin homologues and (unlike stomatin) is fully extractable from erythrocyte membrane
53   MEC-8 establishes the canonical long mec-2/Stomatin isoform in touch neurons, but surprisingly the
54                 Whereas neither the central, stomatin-like domain of MEC-2 nor human stomatin retaine
55 onase-like MEC-6 and the cholesterol-binding stomatin-like MEC-2 proteins.
56              Here we examined the ability of stomatin-like protein 1 (STOML1) to modulate the proton-
57                                              Stomatin-like protein 2 (SLP-2) is a mostly mitochondria
58 ate that Parkin interacts with mitochondrial Stomatin-like protein 2 (SLP-2), which also binds the mi
59 romatography and tandem mass spectrometry as stomatin-like protein 2 (Stoml2), previously described a
60 T6) and one putative novel asthma risk gene, stomatin-like protein 2 (STOML2).
61 and unusual stomatin homologue, human SLP-2 (stomatin-like protein 2).
62 on), suppresses three phenotypes of neuronal stomatin-like protein deficiency as follows: volatile an
63 lone molecules, it has now been shown that a stomatin-like protein regulates a gap junction channel i
64  and functions synergistically with MEC-2 (a stomatin-like protein that regulates MEC-4(d)/MEC-10(d)
65                           unc-1(dn) alters a stomatin-like protein that regulates unc-9 electrical si
66                                  Loss of the stomatin-like protein UNC-1, which is a regulator of UNC
67                                     A second stomatin-like protein, UNC-24, colocalizes with MEC-2 in
68 anically gated ion channels is controlled by stomatin-like protein-3 (STOML3), which is required for
69 re frequently associated with genes encoding stomatin-like proteins (slipins).
70 enome contains two paralogous genes encoding stomatin-like proteins (SLPs; AtSLP1 and AtSLP2) that ar
71 y that similar ion channels may be formed by stomatin-like proteins and DEG/ENaC proteins that are co
72                               These neuronal stomatin-like proteins are putative chaperone proteins t
73 cate that modulation of DEG/ENaC channels by stomatin-like proteins is evolutionarily conserved and m
74 d ssu-1 is the first association of neuronal stomatin-like proteins sharing regulatory roles with a s
75                                 The neuronal stomatin-like proteins UNC-1 and UNC-24 play important r
76                                          The stomatin-like region of MEC-2 interacts with the intrace
77 e integral membrane protein MEC-2 contains a stomatin-like region that is highly conserved from bacte
78                                              Stomatin-like regions in other proteins may serve a simi
79 eract with the MEC-4 degenerin through their stomatin-like regions, which act as protein binding doma
80     Thus, like caveolin-1 and flotillin-1, a stomatin may also associate with non-clathrin coated, DR
81 channel subunit MEC-4 and channel-associated stomatin MEC-2 are specifically required for neural resp
82 ndings provide a molecular framework for how Stomatin oligomers shape membrane architecture and mecha
83           We hypothesize that SLP-2 may link stomatin or other integral membrane proteins to the peri
84 es that are membrane raft associated, namely stomatin, paraslipin (previously SLP-2) and flotillin.
85                                  Loss of the stomatin/PHB/flotillin/HflK/C (SPFH) domain containing p
86 , as with the erythrocyte lipid raft protein stomatin, podocin is present in high-order oligomers and
87                                              Stomatin potently reduced acid-evoked currents generated
88 f the Flotillin protein complex, part of the Stomatin, Prohibitin, Flotillin, and HflK/C (SPFH) super
89                   AtHIR proteins contain the stomatin/prohibitin/flotillin/HflK/C domain (also known
90 l similarities were found between FliL-C and stomatin/prohibitin/flotillin/HflK/C domains of scaffold
91 rug resistance proteins, and proteins of the stomatin/prohibitin/hypersensitive response family, sugg
92 d' form shows very leaky cells and the 32 kD stomatin protein is missing, although the gene is not mu
93 yed a greater association with flotillin and stomatin, proteins known to associate with sphingolipid-
94 s a contributor to vector competence through Stomatin-regulated cholesterol homeostasis.
95 dentified in nonerythroid tissues, and other stomatin related proteins are found in Drosophila, Caeno
96                                     MEC-2, a stomatin-related protein needed for touch sensitivity, i
97                        Furthermore, blocking stomatin restricted cholesterol availability to the bact
98 ral, stomatin-like domain of MEC-2 nor human stomatin retained the activity of full-length MEC-2, bot
99                            We also show that stomatin's mobility on the plasma membrane changes durin
100 unc-24, named ssu-1(fc73) (for suppressor of stomatin uncoordination), suppresses three phenotypes of
101                                       Ixodes stomatin was experimentally validated as a bona fide ATF
102     To establish the identity of the signal, stomatin was fractionated by combinations of cation exch
103                                   Band 3 and stomatin, which reflect the bulk mass of erythrocyte DRM
104 phb1, Zm-phb2, Zm-phb3, and Zm-phb4), one to stomatins (Zm-stm1), and three to a gene implicated in p

 
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